Lead the CQV Program at BIOVECTRA ensuring compliance in a full time role. Oversee commissioning and qualification of Facilities, Utilities, and Equipment while maintaining validated states throughout their lifecycle.

As a CQV Supervisor, you will provide technical leadership within a dynamic team at BIOVECTRA. Collaborate cross-functionally with multiple departments including Engineering, Manufacturing, and Quality to support compliance and continuous improvements. This role demands expertise in GMP systems and hands-on experience in commissioning and qualification.

Key Responsibilities:
• Lead Facilities, Utilities, and Equipment CQV Program
• Develop and maintain CQV schedules and prioritize activities




• Plan and oversee lifecycle management activities
• Review and approve various CQV documentation
• Monitor regulatory compliance and implement improvements

Requirements:
• Bachelor’s degree in a technical discipline
• Minimum three years in a GMP environment
• Experience in CQV, validation, and quality systems
• Strong technical writing and problem-solving skills
• Supervisory experience is a plus

Elevate the CQV program by using your leadership and technical expertise in this vital role at BIOVECTRA.
#J-18808-Ljbffr

📌 CQV Supervisor at BIOVECTRA (Nova Scotia)
🏢 Agilent Technologies
📍 Nova Scotia